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This research is studying a device already approved by the Food and Drug Administration (FDA) to treat wound closures. Researchers are studying a large group of people to continue to learn information about the safety of the STRATAFIX suture and how people's bodies react to using it over a long period of time. This research will provide additional information about using STRATAFIX sutures to close surgical wounds.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
University of Michigan Health Sparrow
Lansing, Michigan, United States
Start Date
November 1, 2025
Primary Completion Date
June 30, 2026
Completion Date
December 31, 2026
Last Updated
November 5, 2025
160
ESTIMATED participants
STRATAFIX PDS and Monocryl suture
DEVICE
Lead Sponsor
University of Michigan
Collaborators
NCT06962215
NCT07478289
NCT06528288
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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